Taiwan FDA registration 6af4836b2f8789bb0a5a26014882e77e
“Genoss” PTCA Balloon Catheter
TW: “吉諾司”冠狀動脈球囊導管
Taiwan·Risk Class 2·MD·Genoss Co., Ltd.·Registered Jan 22, 2020 – Jan 22, 2025ExpiredRegistration details
- Analysis ID
- 6af4836b2f8789bb0a5a26014882e77e
- License Form
- Ministry of Health Medical Device Import No. 033226
- Customs Code
- DHA05603322602
Company information
- Manufacturer
- Genoss Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- EMERGO TAIWAN LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E0005 Percutaneous puncture of the coronary ductus
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 22, 2020
- Expiry Date
- Jan 22, 2025
About this record
Access comprehensive regulatory information for “Genoss” PTCA Balloon Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6af4836b2f8789bb0a5a26014882e77e and manufactured by Genoss Co., Ltd.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.
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